Tecnilatex S.A. is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Tecnilatex S.A. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Tecnilatex S.A. has 1 FDA 510(k) cleared medical devices. Based in Madrid, ES.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Tecnilatex S.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tecnilatex S.A.
1 devices